Peter M. Rothenberg, M.D.
Country not established
- Devices
- 1
What Peter M. Rothenberg, M.D. makes
The company designs a temporary transvenous pacemaker placement assist device, which aids in the precise insertion of temporary pacing leads during cardiac procedures.
This device is classified as Class II under FDA regulations and is listed in the 510(k) clearance registry. The manufacturer is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Peter M. Rothenberg, M.D. have in the registry?
The registry currently lists 1 device for Peter M. Rothenberg, M.D.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Peter M. Rothenberg, M.D.'s devices?
Among its 1 most recently registered device, Peter M. Rothenberg, M.D. has devices listed in FDA 510(k) (1 device).
What risk classes do Peter M. Rothenberg, M.D.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Peter M. Rothenberg, M.D.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Peter M. Rothenberg, M.D. in the registry?
The most recently registered devices listed for Peter M. Rothenberg, M.D. include TEMPORARY TRANSVENOUS PACEMAKER PLACEMENT ASSIST DEVICE.